Serves as a resource for best practices in managing major clinical trials, working independently with minimal supervision. Provides guidance on both study and device trials, oversees implementation of new protocols, and supports regulatory compliance. Coordinates with investigators, sponsors, and regulatory staff to resolve challenges, ensure timely IRB submissions, and support effective trial operations.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Mid Level